Two-part adhesive and bonding method employing same

ABSTRACT

A two-part adhesive comprising an aqueous emulsion adhesive and a gelling agent, which can bond without any temporary tacking or fixing means, and a method for bonding with said two-part adhesive.

This application is a continuation-in-part application of U.S. Ser. No.122,702 filed on Feb. 19, 1980, now abandoned.

The present invention relates to a two-part adhesive and a method forbonding with an aqueous emulsion adhesive. More particularly, it relatesto a two-part adhesive comprising an aqueous emulsion adhesive and agelling agent which can bond instantaneously, and a method for bondingwith the two-part adhesinve.

There have hitherto been known various adhesives which contain anorganic solvent as a medium, but such organic solvent type adhesiveshave unfavorably some problems such as flammability, toxicity, andenvironmental pollution. Accordingly, there have recently been usedaqueous emulsion adhesives, when either one or both of substances to beadhered are a substance which can permeate and absorb water or steam.

The aqueous emulsion adhesives usually comprise an emulsion of a polymerin water and optionally a tackifier, a filler, a plasticizer, acolorant, an aging inhibitor, or the like. The aqueous emulsionadhesives have no flammability and a low toxicity and hence are safe andhygienic, and further they can be filled well because of the lowviscosity (while they have a high nonvolatile content) and can bediluted with water. However, the aqueous emulsion adhesives haveunfavorably a low initial bond strength in comparison with organicsolvent type adhesives, and hence, much time is required until thesufficient bond strength is achieved. For instance, when a thermalinsulator such as a polyurethane foam is bonded onto a steel board ofthe car ceiling, they can be bonded with organic solvent type adhesivesonly by applying the adhesives to surface of the steel board and/orthermal insulator and assembling them under pressure, i.e. only by acontact pressing, but in case of using aqueous emulsion adhesives, thethermal insulator is peeled off and falls with its weight unless thethermal insulator is temporarily tacked or fixed with any other meansuntil the adhesive cures, i.e. an extra step of the temporary tacking orfixing is required after the contact pressing.

In order to eliminate of the drawback of the aqueous emulsion adhesives,it has been studied to improve the initial bond strength of aqueousemulsion adhesives and thereby to achieve rapidly the desired bonding.For instance, it is necessary to increase the viscosity of the adhesiveby increasing the amount of the solid components thereof, or to heat thesubstances to be bonded before or after the application of the adhesivein order to distill water contained in the substances. According tothese methods, however, the storage stability and/or applicationperformances of the adhesives are deteriorated, or another apparatus isrequired. Thus, there has never been found any satisfactorily improvedmethod.

Under the circumstances, the present inventors have intensively studiedon an improvement of aqueous emulsion adhesives. As a result, it hasbeen found that when the aqueous emulsion adhesive is used in acombination of a gelling agent, the aqueous emulsion adhesive caninstantaneously exhibit an initial bond strength and the substances tobe bonded can sufficiently be bonded without any other temporary tackingor fixing means.

An object of the present invention is to provide an improved aqueousemulsion adhesive in the form of a kit of an aqueous emulsion adhesiveand a gelling agent, i.e. an improved two-part adhesive. Another objectof the invention is to provide a method for bonding with the two-partadhesive as set forth above. A further object of the invention is toprovide a method for applying the two-part adhesive to the substances tobe bonded. These and other objects and advantages of the invention willbe apparent to persons skilled in the art from the followingdescription.

According to the present invention, both of the gelling agent and theaqueous emulsion adhesive are simultaneously applied to the substancesto be bonded. That is, both of the gelling agent and the aqueousemulsion adhesive are each sprayed and thereby mixed in the state ofmist, and then applied to the substances to be bonded. That is, thegelling agent and the aqueous emulsion adhesive are each simultaneouslysprayed onto either one or both of the substances to be bonded so thatthe spraying areas of both the gelling agent and aqueous emulsionadhesive are overlapped, and thereafter, the substances to be bonded arepiled up and a pressure is given thereon. The spraying machine is notlimited and includes any machine which can spray both the gelling agentand aqueous emulsion adhesive so that the spraying areas are overlapped,for example using two spray guns which are regulated so that the bothspraying areas are overlapped, or a spray gun having two spray nozzles(e.g. 69 GW PLURAL COMPONENT SPRAY GUN, made by Binks ManufacturingCompany, in U.S.A.). Alternatively, both the gelling agent and aqueousemulsion adhesive may simultaneously be sprayed from air nozzle andfluid nozzle respectively by using one spray gun.

The gelling agent used in the present invention, which can gelate theaqueous emulsion adhesive, includes various surface active agents whichcan neutralize the surface charge of particles of emulsion contained inthe aqueous emulsion adhesives, metal hydroxides, organic acids, organicacid salts, inorganic acid salts, water glass, and water-soluble organicsolvents. As the gelling agent, there may also be used emulsions havingan opposite charge of that of the aqueous emulsion adhesives, whichmeans, for example, the case that when an anionic aqueous emulsionadhesive is used, a cationic emulsion is used as the gelling agent.

Suitable examples of the surface active agents are cationic surfaceactive agents, such as salts of primary, secondary or tertiaryalkylamines (e.g. laurylamine hydrochloride, dilaurylaminehydrochloride, lauryldimethylamine hydrochloride), alkanolamine salts(e.g. ethanolamine hydrochloride), polyethylenepolyamine salts (e.g.ethylenediamine hydrochloride, diethylenetriamine hydrochloride),quaternary ammonium salts (e.g. alkyltrimethylammonium hydrochloride),alkaline nitrogen-containing compounds (e.g. morpholine, guanidine,hydrazine, N,N-diethylenediamine, aminoethylethanolamine); anionicsurface active agents, such as carboxylic acid salts (e.g. sodiumlaurate, sodium oleate, sodium stearate), higher alcohol sulfate salts,higher alkylpolyethyleneglycol sulfate salts, α-olefin sulfate salts,alkylbenzene sulfonate salts, α-olefin sulfonate salts, succinic acidsulfonate salts, higher alcohol phosphate salts, dithiophosphate salts;ampholytic surface active agents, such as carboxylic acid salt typeampholytic surface active agent (e.g. methyl laurylaminopropionatehydrochloride, lauryldimethylbetaine), and other ampholytic surfaceactive agents of various types such as sulfate salts, sulfonate salts,phosphate salts, or the like.

Suitable examples of the metal hydroxides are calcium hydroxide, sodiumhydroxide, potassium hydroxide, or the like. Suitable examples oforganic acids are malic acid, citric acid, oxalic acid, lactic acid, andvarious amino acids. Suitable examples of the organic acid salts aresodium oxalate, calcium acetate, magnesium acetate, calciumpantothenate, and various amino acid salts such as glycine calcium salt,alanine calcium salt, serine calcium salt, threonine calcium salt,methionine calcium salt, phenylalanine calcium salt, calcium aspartate.Suitable examples of the inorganic acid salts are sodium chloride,potassium chloride, potassium bromide, sodium sulfate, aluminum sulfate,magnesium sulfate, copper sulfate, zinc sulfate, ferric sulfate, ferroussulfate, calcium chloride, zinc chloride, magnesium chloride, aluminumchloride, magnesium carbonate, alum, metal primary phosphates (e.g.calcium primary phosphate, magnesium primary phosphate, zinc primaryphosphate) or the like. Suitable examples of the water-soluble organicsolvents are alcohols (e.g. methanol, ethanol, isopropanol), ketones(e.g. acetone, methyl ethyl ketone), or the like.

These gelling agent may be used alone or in a combination of two or morethereof. The most suitable gelling agent can be selected in view of thecomponents and characteristics of the aqueous emulsion adhesives,characteristics of the substances to be bonded and the applicationmanners. Since the less corrosive action to the spraying machine, lesseffect onto human body, significant gelling effect, or the like, thecarboxylic acid salt type surface active agents and organic acid saltsare preferred. In case of using aqueous emulsion adhesive havingcarboxyl or methylol group, polyvalent metal salts of the organic acidsor inorganic acids and polyvalent metal hydroxides (polyvalent metalmeans a metal having two or more valences) are preferable because theycan give excellent bonding with improved heat resistance and waterresistance. A polyfunctional epoxy compound may preferably beincorporated in order to improve the heat resistance and waterresistance of the bonding. A combination of an organic acid salt orinorganic acid salt with a surface active agent is also preferable. Inview of less toxicity to human body, amino acid salts and pantothenicacid salt are particularly preferable.

In case of using anionic aqueous emulsion adhesives, it is alsopreferable to use organic acid metal salts, inorganic acid metal salts,or metal hydroxides as the gelling agent, and further, in case of usingcationic aqueous emulsion adhesives, it is preferable to use anionicsurface active agents, organic acids, inorganic acids, organic acidsalts, inorganic acid salts or water glass as the gelling agent, becausethey can give particularly high initial bond strength. When organic acidmetal salts, carboxylic acid type surface active agents, phosphate typeampholytic surface active agents, metal hydroxides, organic acid metalsalts or primary phosphoric acid metal salts, particularly primaryphospharic acid metal salts are used as the gelling agent, there can beobtained bonding with excellent anticorrosive properties.

The gelling agents are preferably used in the form of an aqueoussolution, particularly an aqueous solution having a solid component of0.5 to 50% by weight. If it is desirable to exhibit more rapidly theinitial bond strength, an organic solvent solution may be used. Theaqueous or organic solvent solution may be prepared when used.

The amount of the gelling agents is not critical and may vary with thekinds of the gelling agents, the aqueous emulsion adhesives and thesubstances to be bonded, but is usually in the ratio of the aqueousemulsion adhesive:the gelling agent=100:0.005 to 100:5 by weight (as thesolid component). Besides, when an emulsion is used as the gellingagent, the ratio of the aqueous adhesive:the gelling agent=1:0.01 to1:100 by weight is preferable. The application amount of the aqueousemulsion adhesive and gelling agent is preferably in the rage of 50 to300 g/cm² in total.

The aqueous emulsion adhesives used in the present invention include allaqueous emulsion adhesives, for example, emulsions containing as themain solid component polyvinyl acetate, vinyl acetate copolymer,polyacrylate, acrylate copolymer, ethylene/vinyl acetate copolymer,polyolefin, styrene/butadiene copolymer, methyl methacrylate/butadienecopolymer, nitrile/butadiene copolymer, polychloroprene, polyisoprene,polyurethane, polyepoxyasphalt, styrene/isoprene copolymer, maleicacid/isoprene copolymer sodium salt, polyvinyl chloride, vinylidenechloride copolymer, polyvinylpyrrolidone, polyvinyl alkyl ether,phenol-formalin reaction mixture, or the like. The emulsions mayoptionally contain tackifiers (e.g. rosin, denatured phenyl resin,terpene, petroleum resin, coumarone/indene resin), fillers (e.g. calciumcarbonate, cley, silica, asbestos), plasticizers (e.g. higher alcohol,glycol, phthalic acid ester), colorants (e.g. titanium white, otherdyestuffs or pigments), aging resistant agents (e.g. antioxidants,ultraviolet absorbers, acid absorbers), or the like. The emulsionscontain a solid component of 15 to 75% by weight.

The two-part adhesive of the present invention is applicable to bond anysubstances, particularly substances, one of which can permeate or absorbwater or steam and another one of which can not permeate or absorb wateror steam. For instance, it is useful for bonding a polyurethane foamwith a steel panel or plate.

The present invention is illustrated by the following Preparations andExamples, but is not limited thereto.

PREPARATION 1

    ______________________________________                                        Al.sub.2 (SO.sub.4).sub.3.18H.sub.2 O                                                         10% by weight                                                 Water           90% by weight                                                 ______________________________________                                    

The above components are mixed with agitation to give a gelling agent.

PREPARATIONS 2 TO 7

Various gelling agents are prepared by using the components shown inTable 1 in the same manner as described in Preparation 1. In Table 1,the amount of the components is % by weight.

                  TABLE 1                                                         ______________________________________                                                     Preparation No.                                                  Components     2     3       4   5     6   7                                  ______________________________________                                        Calcium acetate                                                                              10    --      --  --    --  --                                 Ca(CH.sub.3 COO).sub.2.2H.sub.2 O                                             Zinc acetate   --     5      --  --    --  --                                 Zn(CH.sub.3 COO).sub.2.2H.sub.2 O                                             Magnesium chloride                                                                           --    --      10  --    --  --                                 MgCl.sub.2.6H.sub.2 O                                                         Glacial acetic acid                                                                          --    --      --   5    --  --                                 Phosphoric acid                                                                              --    --      --  --    10  --                                 Alkylbenzenedimethyl-                                                                        --    --      --  --    --  10                                 ammonium chloride                                                             (Sanisol B-50, made by                                                        Kao Atlas)                                                                    Water          90    95      90  95    90  90                                 ______________________________________                                    

PREPARATIONS 8 TO 15

Various gelling agents are prepared by using the components shown inTable 2 in the same manner as described in Preparation 1. In Table 2,the amount of the components is % by weight.

                  TABLE 2                                                         ______________________________________                                                     Preparation No.                                                  Components     8     9     10   11  12  13  14   15                           ______________________________________                                        Calcium pantothenate                                                                         10    --    --   --  --  --  --   --                           Glycine calcium salt                                                                         --    10    --   --  --  --  --   --                           Alanine calcium salt                                                                         --    --    10   --  --  --  --   --                           Serine calcium salt                                                                          --    --    --   10  --  --  --   --                           Threonine calcium salt                                                                       --    --    --   --  10  --  --   --                           Methionine calcium salt                                                                      --    --    --   --  --  10  --   --                           Phenylalanine calcium salt                                                                   --    --    --   --  --  --  10   --                           Calcium aspartate                                                                            --    --    --   --  --  --  --   10                           ______________________________________                                    

EXAMPLE 1

An anionic type acrylate copolymer emulsion adhesive (Penguin Bond No.136, made by Sunstar Chemical Industry Co.,) and the gelling agentprepared in Preparation 1 (100:2 by weight) were applied to apolyurethane foam (made by MTP Chemical Co., 5×50×150 mm, foamingextent: 50-fold) in an amount of about 150 g/m² with a spray gun havingtwo spray nozzles (69 GW Spray Gun, made by Binks Manufacturing Co.).After drying for a fixed time as shown in Table 2, a coated steel plate(coated with melamine alkyd, 200×50×0.8 mm) was piled up thereon, andwas pressed with hand.

Immediately after the above contact pressing, the adhered product washorizontally kept so that the polyurethane foam became underside, and aweight of 50 g was given to one end of the polyurethane foam, and therewas measured the time until the polyurethane foam was peeled off in thewidth of 100 mm. The test was done at 20° C. and a relative humidity of65%. As a reference, the test was done in case of using no gellingagent. The results are shown in Table 3.

                  TABLE 3                                                         ______________________________________                                               Drying time (Second)                                                   Test Product                                                                           5       60        300   420     600                                  ______________________________________                                        Example 1                                                                              ∞ ∞   ∞                                                                             ∞ ∞                              Reference                                                                              0 sec.  0 sec.    5 sec.                                                                              15 sec. 30 sec.                              ______________________________________                                    

In the above test, in case of the product of Example 1, the peeling wasmerely about 5 mm in all drying times.

EXAMPLE 2

In the same manner as described in Example 1 except that the drying timewas 5 seconds, a polyurethane foam and a steel plate were bonded byusing the gelling agents prepared in Preparation 2 to 7, and theproducts thus obtained were subjected to the test of peeling likewise.As a reference, the test was done in case of using no gelling agent. Theresults are shown in Table 4.

                  TABLE 4                                                         ______________________________________                                        Preparation No.                                                                         2      3     4     5   6     7   Reference                          ______________________________________                                        Time of peeling                                                                         ∞                                                                              ∞                                                                             ∞                                                                             50  45    ∞                                                                           0                                  (second)                                                                      ______________________________________                                    

In the above test, in case of the products obtained by using the gellingagents in preparation 2, 3 and 4, the peeling was merely about 5 mm, andin case of that obtained by using the gelling agent in Preparation 7,the peeling was merely about 30 mm.

As is clear from the above results in Table 3 and 4, according to thepresent invention, the desired initial bond strength can be exhibitedonly by drying the coating layer for about 5 seconds, and hence, notemporary fixing is required.

EXAMPLE 3

An anionic type acrylate copolymer emulsion adhesive (Penguin Bond No.136, made by Sunstar Chemical Industry Co.) and the gelling agentsprepared in Preparation 8 to 15 (100:4 by weight) were applied to apolyurethane foam (made by MTP Chemical Co., 5×50×150 mm, foamingextent: 50-fold) in an amount of about 150 g/m² with a spray gun havingtwo spray nozzles (69 GW Spray Gun, made by Binks Manufacturing Co.).After drying for a fixed time as shown in Table 5, a coated steel plate(coated with melanine alkyd, 200×50×0.8 mm) was piled up thereon, andwas pressed with hand.

Immediately after the above contact pressing, the adhered product washorizontally kept so that the polyurethane foam became underside, and aweight of 50 g was given to one end of the polyurethane foam, and therewas measured the time until the polyurethane foam was peeled off in thewidth of 100 mm. The test was done at 20° C. and a relative humidity of65%. As a reference, the test was done in case of using no gellingagent. The results are shown in Table 5.

                  TABLE 5                                                         ______________________________________                                                  Drying time (second)                                                Test product                                                                              5        60    300     420  600                                   ______________________________________                                        Preparation 8                                                                             ∞  ∞                                                                             ∞ ∞                                                                            ∞                               Preparation 9                                                                             "        "     "       "    "                                     Preparation 10                                                                            "        "     "       "    "                                     Preparation 11                                                                            "        "     "       "    "                                     Preparation 12                                                                            "        "     "       "    "                                     Preparation 13                                                                            "        "     "       "    "                                     Preparation 14                                                                            "        "     "       "    "                                     Preparation 15                                                                            "        "     "       "    "                                     Reference   0        0     5       15   30                                    ______________________________________                                    

In the above test, in case of the product of Preparation 8 to 15, thepeeling was merely about 5 mm in all drying times.

As is clear from the above results in Table 5, according to the presentinvention, the desired initial bond strength can be exhibited only bydrying the coating layer for about 5 seconds, and hence, no temporaryfixing is required.

EXAMPLE 4

An anionic type acrylate copolymer emulsion adhesive (Penguin Bond No.136, made by Sunster Chemical) and the gelling agents prepared inPreparation 8 to 15 (100:4 by weight) were applied to a steel plate(0.8×50×150 mm) in an amount of about 150 g/m² with a spray gun havingtwo spray nozzles (69 GW Spray Gun, made by Binks Manufacturing Co.).

After drying at 20° C. and a relative hymidity of 60% for 24 hours, theproducts were subjected to the test of anticorrosive property in waterat 20° C. for 24 hours. The results are shown in Table 6.

                  TABLE 6                                                         ______________________________________                                        Preparation No.                                                                         8      9     10    11  12    13  14    15                           ______________________________________                                        anticorrosive                                                                           ○                                                                             ○                                                                            ○                                                                            ○                                                                          ○                                                                            ○                                                                          ○                                                                            ○                     property                                                                      ______________________________________                                         ○: good,                                                               x: poor                                                                  

EXAMPLE 5

The gelling agents prepared in Preparations 8 to 15 were applied to apolyurethane foam (80×80×4 mm, foaming extent: 50-fold, made by MTPChemical Co.) in an amount of 50 g/m² with air spray and the coatinglayer was dried at room temperature for 24 hours.

A polyacrylate emulsion adhesive (Penguin Bond No. 135, made by SunstarChemical Industry Co.) was applied to a coated steel plate (coated withmelamine alkyd, 100×100×0.8 mm) in an amount of 100 g/m² with airlessspray. After 30 seconds, the steel plate was piled up with thepolyurethane foam prepared above with facing the coating layers, and theresultant was rolled with a roller of 1 kg. After 30 seconds, the bondedproduct was subjected to a test for tensile strength in verticaldirection to the bonding face with an autograph machine (IS-500, made byShimazu Seisakusho) under the conditions of a rate of pulling: 500mm/minute, a temperature: 20° C., and a relative humidity: 60%.

The results are shown in Table 7.

                  TABLE 7                                                         ______________________________________                                        Gelling agents                                                                              Tensile strength (g/cm.sup.2)                                   ______________________________________                                        Preparation 8 58.0                                                            Preparation 9 60.5                                                            Preparation 10                                                                              47.3                                                            Preparation 11                                                                              39.5                                                            Preparation 12                                                                              43.7                                                            Preparation 13                                                                              30.4                                                            Preparation 14                                                                              39.6                                                            Preparation 15                                                                              64.0                                                            ______________________________________                                    

As is clear from the above test results, when the gelling agents of thepresent invention are used, the initial bond strength is rapidlyexhibited, and hence, when this method is employed, the polyurethanefoam can be bonded to the ceiling of a motor car without any temporaryfixing.

EXAMPLE 6

The gelling agents prepared in Preparations 8-15 were applied to apolyurethane foam (140×100×5 mm) in an amount of 100 g/m² with airspray, and the coating layer was dried at 20° C. and a relative humidityof 60% for 24 hours.

A polyacrylate emulsion adhesive (Penguin Bond No. 135) was applied to asteel plate (140×100×0.7 mm) in an amount of 100 g/m² with air spray,and the resultant was allowed to stand at 20° C. and relative humidityof 60% for 1 minute, and thereafter, the steel plate thus coated waspiled up with the polyurethane foam obtained above and pressed withhand. After 2 minutes, the resulting product was subjected to the testfor tensile strength with an autograph machine in the same manner asdescribed in Example 5. The results are shown in Table 8.

                  TABLE 8                                                         ______________________________________                                        Gelling agents                                                                              Tensile strength (g/cm.sup.2)                                   ______________________________________                                        Preparation 8 105                                                             Preparation 9 110                                                             Preparation 10                                                                              80                                                              Preparation 11                                                                              75                                                              Preparation 12                                                                              86                                                              Preparation 13                                                                              69                                                              Preparation 14                                                                              81                                                              Preparation 15                                                                              120                                                             ______________________________________                                    

EXAMPLE 7

The gelling agent prepared in Preparation 15 was applied to a needledfelt (80×80×4 mm) in an amount of 50 g/m² with spray, and dried at roomtemperature for 24 hours.

A carboxyl-modified SBR latex adhesive (Penguin Bond No. 551, made bySunster Chemical Industry Co.) was applied to a coated steel plate(coated with melamine alkyd, 100×100×0.8 mm) in an amount of 150 g/m²with airless spray. After 30 seconds, the steel plate was piled up withthe coated felt prepared above with facing the coating layers, androlled with a roller of 1 kg. After allowing to stand for 30 seconds and300 seconds, the product thus obtained was subjected to a test fortensile strength in the same manner as described in Example 5. Theresults are shown in Table 9.

                  TABLE 9                                                         ______________________________________                                        Time of allowing                                                                             Tensile strength (g/cm.sup.2)                                  to stand (seconds)                                                                           Example 3  Reference*                                          ______________________________________                                        30             65.0       0.94                                                300            120.0 (M.F.)                                                                             1.6                                                 ______________________________________                                         *In Reference, no gelling agent was employed.                            

As is clear from the above test results, in case of the presentinvention, the bond strength is increased with lapse of time.

EXAMPLE 8

The gelling agent prepared in Preparation 15 was applied to the knittedcloth of a polyvinyl chloride leather with knitted back cloth in anamount of 50 g/m² with air spray and dried at room temperature for 1hour or 24 hours.

A polyacrylate emulsion adhesive (Penguin Bond No. 135) was applied tothe same coated steel plate as used in Example 7 in an amount of 150g/m² with air spray, and after 30 seconds, it was piled up with theleather prepared above with facing the coating layers, and then rolledwith a roller of 1 kg.

After allowing to stand for 30 seconds and 300 seconds, the product wassubjected to the test of tensile strength in the same manner asdescribed in Example 5. The results are shown in Table 10.

                  TABLE 10                                                        ______________________________________                                                  Tensile strength (g/cm.sup.2)                                                   Example 4                                                                     Time of drying of the                                             Time of allowing                                                                          gelling agent (hour)                                              to stand (seconds)                                                                        1           24       Reference                                    ______________________________________                                        30          34.6        47.2     0.00                                         300         132.8       139.1    0.78                                         ______________________________________                                    

As is clear from the above test results, the bond strength is furtherimproved with prolonging the time of drying of the gelling agent.

What is claimed is:
 1. A method for bonding two substances togetherwhich comprises applying a two-part adhesive comprising an aqueoussynthetic resin emulsion adhesive and a gelling agent selected from thegroup consisting of calcium pantothenate, glycine calcium salt, alaninecalcium salt, serine calcium salt, threonine calcium salt, methioninecalcium salt, phenylalanine calcium salt, and calcium aspartate to atleast one of the substances to be adhered, disposing the substances oneon the other, and then contact-pressing them together.
 2. A methodaccording to claim 1, wherein the aqueous synthetic resin emulsionadhesive and the gelling agent are simultaneously applied to thesubstances to be bonded in the form of spray.
 3. A method according toclaim 1, wherein the gelling agent is used in the form of a 0.5 to 50%by weight aqueous solution.
 4. A method according to claim 1, whereinthe aqueous synthetic resin emulsion adhesive and the gelling agent areused in the ratio of 100:0.005 to 100:5 by weight (as the solidcomponent).
 5. A two-part adhesive comprising an aqueous synthetic resinemulsion and a gelling agent selected from the group consisting ofcalcium pantothenate, glycine calcium salt, alanine calcium salt, serinecalcium salt, threonine calcium salt, methionine calcium salt,phenylalanine calcium salt, and calcium aspartate.
 6. A two-partadhesive according to claim 5, wherein the aqueous synthetic resinemulsion is an aqueous emulsion containing as the main solid component apolymer selected from the group consisting of polyvinyl acetate, vinylacetate copolymer, polyacrylate, acrylate copolymer, ethylene/vinylacetate copolymer, polyolefin, styrene/butadiene copolymer, methylmethacrylate/butadiene copolymer, nitrile/butadiene copolymer,polychloroprene, polyisoprene, polyurethane, polyepoxyasphalt,styrene/isoprene copolymer, maleic acid/isoprene copolymer sodium salt,polyvinyl chloride, vinylidene chloride copolymer, polyvinylpyrrolidone,polyvinyl alkyl ether, and phenol-formalin reaction mixture.